Human Gene Set: WP_SMITH_MAGENIS_AND_POTOCKI_LUPSKI_SYNDROME_COPY_NUMBER_VARIATION


Standard name WP_SMITH_MAGENIS_AND_POTOCKI_LUPSKI_SYNDROME_COPY_NUMBER_VARIATION
Systematic name M48089
Brief description Smith Magenis and Potocki Lupski syndrome copy number variation
Full description or abstract  
Collection C2: Curated
      CP: Canonical Pathways
            CP:WIKIPATHWAYS: WikiPathways
Source publication  
Exact source WP5381
Related gene sets  
External links https://www.wikipathways.org/instance/WP5381
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Source species Homo sapiens
Contributed by WikiPathways
Source platform or
identifier namespace		 Human_NCBI_Gene_ID
Dataset references  
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Global Cancer Map (Broad Institute)
NCI-60 cell lines (National Cancer Institute)
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Show members (show 159 source identifiers mapped to 159 genes)
Version history 2023.2.Hs: First Introduced.

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